A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5469053



Internal ID246846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:19615771..19644254hg38UCSC Ensembl
chr7:19655394..19683877hg19UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg3828484
hg1928484
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16994494
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5469053
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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